[身材矮小伴全垂体功能减退症患者低钠血症致意识丧失]。

K Notsu, C Takagi, I Umaki
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摘要

1994年3月,一名身材矮小(141厘米)的昏迷妇女住进我院。她有低钠血症(120 mEq/l),分娩时大出血。胰岛素诱导的低血糖后,血浆ACTH和皮质醇水平均未升高。然而,反复肌内注射ACTH后,尿17OHCS水平逐渐升高。血浆游离T3和游离T4水平低。静脉注射TRH后血浆TSH和催乳素(PRL)水平均未升高。基础血浆LH、FSH和生长激素(GH)水平较低,对任何刺激试验均无明显反应。脑下垂体的核磁共振成像显示一个空的蝶鞍。这些结果显示她患有全垂体功能减退症,原发性空蝶鞍。开始糖皮质激素替代治疗,血清钠水平立即恢复正常。同时给予左甲状腺素。她年轻时可能患有垂体侏儒症,产后其他垂体激素逐渐减少,可能导致下丘脑-垂体-肾上腺轴受损。
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[Unconsciousness due to hyponatremia in a patient with short stature with panhypopituitarism].

An unconscious woman of short stature (141 cm) was admitted to our hospital in March, 1994. She had hyponatremia (120 mEq/l) and had experienced massive bleeding during delivery. No increment of either plasma ACTH or cortisol levels was observed after insulin-induced hypoglycemia. However, urinary 17OHCS levels gradually increased after repeated intramuscular injections of ACTH. Plasma free T3 and free T4 levels were low. Neither plasma TSH nor prolactin (PRL) levels increased after an intravenous injection of TRH. Basal plasma LH, FSH and growth hormone (GH) levels were low and there were no observable responses to any of the stimulation tests. A magnetic resonance image (MRI) of her pituitary gland showed an empty sella. These results showed that she had a panhypopituitarism with primary empty sella. Replacement therapy with glucocorticoid was started and serum sodium levels normalized immediately. Levothyroxine was also administered. The possibility of pituitary dwarfism during her youth and a gradual postpartum reduction of other pituitary hormones may have caused an impairment of the hypothalamo-pituitary-adrenal axis.

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[Parathyroid hormone]. [Treatment of hypothalamic-pituitary tumors--experiences at Hiroshima University School of Medicine]. [Future aspects on endocrinology]. [A view of basic endocrinology]. [Comment by a surgeon on Japan Endocrine Society, its past and future].
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